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Multigenic engineering of the chloroplast genome in the green alga Chlamydomonas reinhardtii

机译:绿藻中叶绿体基因组的多粒工程<斜斜岩>衣原体Reinhardtii

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The chloroplast of microalgae such as Chlamydomonas reinhardtii represents an attractive chassis for light-driven production of novel recombinant proteins and metabolites. Methods for the introduction and expression of transgenes in the chloroplast genome (=plastome) of C. reinhardtii are well-established and over 100 different proteins have been successfully produced. However, in almost all reported cases the complexity of the genetic engineering is low, and typically involves introduction into the plastome of just a single transgene together with a selectable marker. In order to exploit fully the potential of the algal chassis it is necessary to establish methods for multigenic engineering in which many transgenes can be stably incorporated into the plastome. This would allow the synthesis of multi-subunit proteins and the introduction into the chloroplast of whole new metabolic pathways. In this short communication we report a proof-of-concept study involving both a combinatorial and serial approach, with the goal of synthesizing five different test proteins in the C. reinhardtii chloroplast. Analysis of the various transgenic lines confirmed the successful integration of the transgenes and accumulation of the gene products. However, the work also highlights an issue of genetic instability when using the same untranslated region for each of the transgenes. Our findings therefore help to define appropriate strategies for robust multigenic engineering of the algal chloroplast.
机译:微藻蛋白如衣原体Reinhardtii的叶绿体代表了一种有吸引力的底盘,用于新型重组蛋白和代谢物的光驱动产生。在氯化体基因组(=塑料)中转基因的引入和表达的方法是良好建立的,已经成功地制备了超过100种不同的蛋白质。然而,在几乎所有报道的情况下,基因工程的复杂性都是低的,并且通常涉及与可选标记一起进入仅单个转基因的塑料。为了充分利用藻类底盘的电位,需要建立多烯工程方法,其中许多转基因可以稳定地掺入塑料中。这将允许合成多亚基蛋白质和引入全新的代谢途径的叶绿体。在这短暂的沟通中,我们报告了涉及组合和串行方法的概念证据,其目的是在C.Reinhardtii叶绿体中合成五种不同的测试蛋白。各种转基因系的分析证实了转基因的成功整合和基因产物的积累。然而,当使用对每个转基因的相同未转换的区域时,该工作也突出了遗传不稳定性问题。因此,我们的研究结果有助于确定藻类叶绿体的鲁棒多簇工程的适当策略。

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